To probe how the aerosol substrate influences heterogeneous polycyclic aromatic hydrocarbon (PAH) oxidation, we investigated the reaction of surface-bound anthracene with gas-phase ozone on phenylsiloxane oil and azelaic acid aerosols under dry conditions in an aerosol how tube with offline analysis of anthracene. The reaction exhibited pseudo-first-order kinetics for anthracene loss, and the pseudo-first-order rate coefficients displayed a Langmuir-Hinshelwood dependence on the gas-phase ozone concentration on both aerosol substrates. The following parameters were found: for the reaction on phenylsiloxane oil aerosols, K-O3 = (1.0 +/- 0.4) x 10(-13) Cm-3 and k(max)(I) = (0.010 +/- 0.003) s(-1); for the reaction on azelaic acid aerosols, K-O3 = (2.2 +/- 0.9) x 10(-15) cm(3) and k(max)(I) = (0.057 +/- 0.009) s(-1), where K-O3 is a parameter that describes the partitioning of ozone to the surface and kI(max) is the maximum pseudo-first-order rate coefficient at high ozone concentrations. The K 03 value for the reaction of surface-bound anthracene and ozone on azelaic acid aerosols is similar to the K-O3 value that we obtained in our previous study for the reaction of surface-bound benzo[a]pyrene and ozone on the same substrate. This finding supports our earlier hypothesis that the substrate influences the partitioning of ozone to the surface irrespective of the organic species (i.e., PAH) adsorbed to it. Preliminary ab initio calculations were performed to investigate whether there is a relationship between the relative binding energies of the ozone-substrate complex and the K-O3 values for the different substrates studied. A comparison between kinetic results obtained on aerosol substrates and thin films is presented.